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Updated: Mar 3, 2026

Broth Microdilution In Vitro Screening: An Easy and Fast Method to Detect New Antifungal Compounds
Published on: February 14, 2018
Antifungal Pharmacokinetics/Pharmacodynamics
Yusuke Yagi1,2, Yukihiro Hamada1
1Department of Pharmacy, Kochi Medical School Hospital.
Optimizing antifungal therapy using pharmacokinetics/pharmacodynamics (PK/PD) is key for invasive fungal infections. Bridging research and practice requires addressing knowledge gaps and variability for better patient outcomes.
Area of Science:
- Pharmacology
- Infectious Diseases
- Clinical Pharmacy
Background:
- Optimizing antifungal therapy with pharmacokinetics/pharmacodynamics (PK/PK) principles is crucial for invasive fungal infections.
- Clinical application faces significant challenges, including knowledge gaps and inter-patient variability.
Purpose of the Study:
- To provide a comprehensive overview of PK/PD in antifungal therapy.
- To bridge basic research and clinical practice by analyzing challenges and future directions.
Main Methods:
- Review of fundamental PK/PD concepts and major antifungal drug classes.
- Analysis of preclinical evidence defining key PK/PD indices.
- Critical evaluation of challenges hindering clinical translation.
Main Results:
- Identified key PK/PD indices: concentration-to-minimum inhibitory concentration ratio, 24-h area under the curve-to-minimum inhibitory concentration ratio, and time above minimum inhibitory concentration.
- Highlighted challenges: knowledge gaps (especially for filamentous fungi), pharmacokinetic variability, TDM limitations, narrow therapeutic windows, and antifungal resistance.
- Discussed current strategies like antifungal stewardship.
Conclusions:
- Effective application of PK/PD principles is vital for personalized antifungal therapies.
- Future directions include prioritizing research, improving TDM, developing novel agents, and enhancing research-clinical collaboration.
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